KEGG   VARIANT: 3192v1
Entry
3192v1                      Variant                                
Name
HNRNPU mutation
Type
Loss of function
Gene
HNRNPU  heterogeneous nuclear ribonucleoprotein U [KO:K12888]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 602869
Network
nt06547  Spliceosome
Disease
H00606  Early infantile epileptic encephalopathy
Reference
  Authors
Carvill GL, Heavin SB, Yendle SC, McMahon JM, O'Roak BJ, Cook J, Khan A, Dorschner MO, Weaver M, Calvert S, Malone S, Wallace G, Stanley T, Bye AM, Bleasel A, Howell KB, Kivity S, Mackay MT, Rodriguez-Casero V, Webster R, Korczyn A, Afawi Z, Zelnick N, Lerman-Sagie T, Lev D, Moller RS, Gill D, Andrade DM, Freeman JL, Sadleir LG, Shendure J, Berkovic SF, Scheffer IE, Mefford HC
  Title
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
  Journal
Nat Genet 45:825-30 (2013)
DOI:10.1038/ng.2646
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